meddevicedb.com FDA Device Reference

HI TECH IMPLANT, HT PHYSIO IMPLANT

K091913 Class I Traditional
Decision Date
2009-10-30
Sponsor / Applicant
By Dental Srl

Technical Specification

510(k) Submission ID K091913
Product Code EKX
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4200
Decision Date 2009-10-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HI TECH IMPLANT, HT PHYSIO IMPLANT received FDA 510(k) clearance under submission number K091913, sponsored by By Dental Srl. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2009-10-30.

Classification & Regulation

This clearance is catalogued under FDA product code EKX and 21 CFR 872.4200, within the Dental review panel as a Class I device.